Works
| Single-stage bilateral derotational osteotomy for congenital radio-ulnar synostosis: Case report |
| Rare coincidence, HLHS accompanied by teratoma |
| A case of focal cortical dysplasia type IIIb associated with dysembryoplastic neuroepithelial tumor |
| A case report of Haddad Syndrome in a male newborn |
| Dysmorphic patient with CHD1 gene variant – case report |
| Association between maternal SARS-CoV-2 infection and fetal Juvenile Xantogranuloma: Case Report |
| Intraoral Atypical Spitzoid Tumor associated with Peutz-Jeghers Syndrome: A Case Report |
| 11 Recurrent Lower Respiratory Tract Infections In Vacter Association Patient- Underlying Cause And Diagnosis Process |
| Neurofibromatosis type-1 Familial Case Report: Importance of Genetic Counselling |
| Caecal Duplication As A Rare Cause Of Acute Abdomen: Case Report |
| Down Syndrome, Leukemia, and Facial Nerve Paralysis – Clinical, Diagnostic, and Therapeutic Analysis of a case of a 3-year-old girl with an exceptional triad of symptoms |
| Many Complications with Pediatric Acute Mastoiditis: A Case Report |
| Difficulties in using therapeutic hypothermia in newborns with congenital anaemia due to fetomaternal haemorrhage – case series |
| Was it only an unfortunate accident? – CASE REPORT |
| Lymphopenia – an essential indicator of SCID |
| Tuberous sclerosis complex – a multisystem disease: Case Report |
| Multisystem Inflammatory Syndrome In Children (Mis-C): Insights From A Clinical Case And Management Strategies |
| 2 sisters with sex developement disorder (DSD) – sex reversal disorder type 3 |